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1. 重庆医科大学基础医学院病理学教研室
2. 重庆医科大学基础医学院病理学教研室,重庆,400016
纸质出版日期:2008,
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[1]姜小良,张徽,刘香丽,林晓.曲古菌素A对乳腺癌MDA-MB-231细胞的作用[J].重庆医科大学学报,2008(03):312-316.
JIANG Xiao-liang. The investigation of effect of trichostatin A to breast cancer MDA-MB-231 cell line[J]. Journal of Chongqing Medical University, 2008,(3):312-316.
[1]姜小良,张徽,刘香丽,林晓.曲古菌素A对乳腺癌MDA-MB-231细胞的作用[J].重庆医科大学学报,2008(03):312-316. DOI: 10.13406/j.cnki.cyxb.2008.03.025.
JIANG Xiao-liang. The investigation of effect of trichostatin A to breast cancer MDA-MB-231 cell line[J]. Journal of Chongqing Medical University, 2008,(3):312-316. DOI: 10.13406/j.cnki.cyxb.2008.03.025.
目的:研究组蛋白去乙酰化酶(Histone deacetylase
HDAC)抑制剂曲古抑菌素A(Trichostatin A
TSA)对乳腺癌细胞MDA-MB-231增殖、侵袭、细胞周期及ERα表达的影响。方法:100~400nmol/L的TSA分别处理MDA-MB-231细胞6~48h后用四甲基偶氮唑蓝比色法(MTT法)检测MDA-MB-231细胞的生长活性。应用流式细胞仪观察细胞周期的变化。采用RT -PCR法检测MDA-MB-231细胞在24h不同浓度100~400nmoi/L TSA作用下对ERα
MMP-9 mRNA表达的影响。采用免疫组织化学法检测MDA-MB-231细胞在24h不同浓度100~400nmol/L TSA作用下对ERα
MMP-9在细胞中表达的影响。采用细胞侵袭实验检测MDA-MB-231细胞在24h不同浓度100~400nmol/L TSA作用下细胞侵袭力的变化。结果:TSA可显著抑制MDA-MB-231细胞的增殖
呈时间及剂量依赖性。TSA能够延缓细胞周期G
2
/M期进程
阻滞细胞于G
2
期。RT-PCR显示
TSA能够上调ERαmRNA在MDA-MB-231细胞中的表达
下调MMP-9在MDA-MB-231细胞中的表达。侵袭实验显示TSA能够较明显的抑制MDA-MB-231细胞的侵袭。结论:TSA能够较明显的上调ERα与下调MMP-9的表达可能是抑制MDA-MB-231细胞增生侵袭与转移的重要机制之一。
Objective:To investigate the influence of histone deacetylase inhibitor(Trichostatin A)to multiplication
invasion
cell cycle of breast cancer MDA-MB-231 cell line.Methods:After 6-48hours treatment with the concentration(100~400nmol/L)of Trichostatin
the growth activity of MDA-MB-231 cell line was detected by MTT.The expression of ERα
MMP-9 mRNA was detected by RT-PCR with different concentration(100~400nmal/L TSA)during 24 hours to MDA-MB-231 cell line.The expression of ERα
MMP-9 protein was examined by immunohistochemistry with different concentration(100~400nmol/L TSA)during 24 hours treatment to MDA-MB-231 cell line.With cell invasion experiment to detect the change of invasive power by using different concentration(100~400nmol/L TSA)during 24 hours to MDA-MB-231 cell line.Results: Trichostatin can inhibit the growth of MDA-MB-231 cell line
which was time and dose dependent.Trichostatin can delay the cell cycle G
2
/M stage
stop the cell stage in G
2
stage.Trichostatin can up-regulate the expression of ERαmRNA
down-regulate the expression of MMP-9 mRNA in cells.The invasion experiment indicate that Trichostatin can conspicuous inhibit the invasion of MDA-MB-231 cell line.Conclusions:Trichostatin can inhibit the accrementition
invasion and metastasis of MDA-MB-231 cell line evidently
and one of the mechanism may be the up-regulation of ERαand the down-regulation of MMP-9.
曲古抑菌素A(TSA)MDA-MB-231细胞雌激素受体α(ERα)基质金属蛋白酶9(MMP-9)
Trichostatin AMDA-MB-231 cell lineEstrogen receptorMatrix metalloproteinases-9
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